BACTERIOPHAGE VIRUS-LIKE PARTICLE VACCINES FOR CHLAMYDIA TRACHOMATIS UROGENITAL INFECTION - PROJECT SUMMARY…
Federal financial assistance recorded from USAspending. This is not a procurement contract.
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ASST_NON_R01AI166360_075 · UNIVERSITY OF NEW MEXICO · Department of Health and Human Services
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- Assistance award identifier
- ASST_NON_R01AI166360_075
- FAIN
- R01AI166360
- Recipient
- UNIVERSITY OF NEW MEXICO
- Awarding agency
- Department of Health and Human Services
- Funding agency
- Department of Health and Human Services
- Assistance listing (CFDA)
- 93.855
- Total obligated
- $1,516,252
- Period
- Dec 6, 2022 – Nov 30, 2027
- Fiscal year
- 2023
- Place of performance state
- NM
- Source file
- FY2023_All_Assistance_Full_20261006.zip
Description
BACTERIOPHAGE VIRUS-LIKE PARTICLE VACCINES FOR CHLAMYDIA TRACHOMATIS UROGENITAL INFECTION - PROJECT SUMMARY CHLAMYDIA TRACHOMATIS IS AN OBLIGATE INTRACELLULAR BACTERIA THAT IS THE MOST COMMON BACTERIAL SEXUALLY TRANSMITTED INFECTION. DESPITE EFFECTIVE ANTIBIOTIC TREATMENT AND SCREENING PROGRAMS, THE PREVALENCE OF CHLAMYDIA CONTINUES TO RISE. ALTHOUGH THE INFECTION CAN BE ASYMPTOMATIC, SOME WOMEN EXPERIENCE SERIOUS LONG-TERM SEQUELAE, INCLUDING PELVIC INFLAMMATORY DISEASE, INFERTILITY, AND ECTOPIC PREGNANCY. FOR THESE REASONS, A PROPHYLACTIC VACCINE AGAINST CHLAMYDIA IS NEEDED. HOWEVER, SIGNIFICANT GAPS EXIST IN OUR KNOWLEDGE OF THE NATURAL IMMUNE RESPONSE TO UROGENITAL CHLAMYDIA TRACHOMATIS INFECTION. IN PARTICULAR, THE SPECIFICITY OF ANTIBODIES ELICITED DURING INFECTION, THEIR FUNCTIONS, AND THEIR PROTECTIVE CAPACITY ARE NOT WELL UNDERSTOOD. THE OVERALL GOAL OF THIS RESEARCH IS TO DESIGN PROPHYLACTIC ANTIBODY-ELICITING VACCINES AGAINST UROGENITAL CHLAMYDIA TRACHOMATIS INFECTION. THE OBJECTIVE OF THIS PROPOSAL IS TO DEFINE THE RANGE OF PROTECTIVE FUNCTIONS ANTIBODIES CAN HAVE AGAINST CHLAMYDIA TRACHOMATIS INFECTION OF THE FEMALE UROGENITAL TRACT, AND USE THIS KNOWLEDGE TO CREATE VACCINES THAT CAN ELICIT THOSE ANTIBODIES. OUR WORKING HYPOTHESIS IS THAT ANTIBODY RESPONSES THAT TARGET PROTEINS KNOWN TO BE INVOLVED IN ADHESION AND ENTRY INTO HOST CELLS OR MEDIATE PATHOLOGY IN THE REPRODUCTIVE TRACT WILL BE PROTECTIVE AGAINST UROGENITAL CHLAMYDIA TRACHOMATIS INFECTION. IN AIM 1, WE WILL ENGINEER EPITOPE-SPECIFIC VACCINE CANDIDATES THAT WILL ELICIT HIGH TITER ANTIBODIES TO CHLAMYDIA TRACHOMATIS ADHESION FACTORS AND DEFINE THEIR IMMUNOGENICITY IN MOUSE IMMUNIZATION STUDIES. IN AIM 2, WE WILL INVESTIGATE THE SPECIFIC FUNCTIONS OF VACCINE-ELICITED ANTIBODIES TO NEUTRALIZE CHLAMYDIA TRACHOMATIS INFECTION IN CELL CULTURE, MEDIATE COMPLEMENT KILLING OF CHLAMYDIA TRACHOMATIS, AND FACILITATE UPTAKE AND KILLING BY NEUTROPHILS. IN AIM 3, WE WILL INVESTIGATE THE PROTECTIVE CAPACITY